FDA inspection

Church & Dwight Manufacturing Co., Ltd.: FDA inspection ending Oct 31, 2017

FDA inspection 1030421 · Voluntary Action Indicated (VAI) · South Chesterfield, VA

Key facts

Inspection ID 1030421
Firm Church & Dwight Manufacturing Co., Ltd.
FEI number 1122329
Address 1851 Touchstone Rd
City South Chesterfield
State VA
ZIP 23834
Country United States
Fiscal year 2018
Inspection end date Oct 31, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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